| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44939874-44940052 | Common:2; Rare:50 | ||||
| chr21:45287877-45288137 | Common:6; Rare:96 | ||||
| chr21:45404934-45405241 | Common:13; Rare:173 | ||||
| chr21:45981543-45981783 | Common:23; Rare:45; Clinvar (benign):1 | ||||
| chr21:46285801-46286047 | Common:1; Rare:56 | ||||
| chr21:46286237-46286399 | Common:4; Rare:60 | ||||
| chr21:46286553-46286697 | Common:1; Rare:47 | ||||
| chr21:46323806-46324222 | Common:3; Rare:157; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458680-46459057 | Common:3; Rare:128 | ||||
| chr21:46635549-46635694 | Common:1; Rare:42 | ||||
| chr22:17628689-17628866 | Common:1; Rare:59 | ||||
| chr22:17638635-17638824 | Rare:71 | ||||
| chr22:17774442-17774613 | Rare:58 | ||||
| chr22:18077785-18078022 | Common:5; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19122382-19122687 | Common:4; Rare:76 |